Adverse events analysis as an educational tool to improve patient safety culture in primary care: an experimental study

Not Applicable

Completed

• Conditions: Patient safety culture; Not Applicable

• Registration Number: ISRCTN41911128
• Lead Sponsor: Department of Health of Galicia (Spain)

Brief Summary

2019 results in https://www.ncbi.nlm.nih.gov/pubmed/30657056 (added 12/02/2020)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2010-12-31
• Study Start: 2011-02-07
• Last Update Posted: 3 March 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 138

Inclusion Criteria

Tutors and residents in Family and Community Medicine in last year of studies in Galicia, Spain

Exclusion Criteria

Unwilling to participate

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> The dependent variable will be patient safety culture as measured by the Hospital Survey on Patient Safety Culture (SOPS). The independent or explanatory variable will be participation in the intervention - training workshops, recording of adverse events in daily work and reception of feedback.<br><br> First round SOPS (3-6 months) and second round SOPS (9-12 months).<br>

Secondary Outcome Measures

Name	Time	Method
<br> Reliability (internal consistency, repeatability), validity (content, criteria, construct) and change sensitivity (size of effect, paired t) of the Hospital Survey on Patient Safety Culture<br><br> First round SOPS (3-6 months) and second round SOPS (9-12 months).<br>